Composition and method for controlled drug release from a tissue

ABSTRACT

A composition, comprising a hydrogel matrix and microparticles within said matrix, said matrix comprising a cross-linkable protein and a cross-linking agent, wherein said cross-linking agent is able to cross-link said cross-linkable protein, wherein said microparticles comprise a drug.

FIELD OF THE INVENTION

The present invention is of a composition and method for controlled drugrelease on a target tissue, and in particular for such a composition andmethod for controlled antibiotic release to an infected tissue or tissuewhich is prone to infection.

BACKGROUND OF THE INVENTION

In several medical situations, infections arise which are difficult totreat using a systemic antibiotic administration. The concentration atthe infected site is too low as a result of poor blood supply, so thatthe drug in the circulation cannot reach the site efficiently. In thiscase increasing the systemic exposure may increase the localconcentration at the site to the desired values; however this approachis prohibited due to the systemic toxicity of the antibiotics, which inmost cases is the limiting factor. A scenario of poor blood supply atinfected sites can arise as a result of tissue trauma or an ensuinginflammation or necrosis. Another medical situation that leads to poortreatment outcomes of systemic antibiotic intervention is thedevelopment of a biofilni. Biofilms are a dense layer of bacteria, whichis made of or encapsulated with a polysaccharide secretion calledglycocalyx. This layer comprises a barrier that shields the bacteriafrom the effect of antibiotics, thus necessitates the use of higher andhigher concentration of these drugs. In addition to the reduced efficacyand danger of toxicity associated with the use of antibiotics to treatsuch infected sites, systemic treatment with antibiotics is the numberone cause in the development of bacterial resistance, and this is anemerging global healthcare concern.

Examples of medical conditions in which local antibiotic therapy ispreferred over systemic exposure include but are not limited toosteomyelitis, bone fractures treated with metal rods, plates orexternal fixators. The risk is especially high with open fractures,total joint replacement, vascular bypass surgery with the use ofartificial graft material, general surgical procedures such as herniarepair and various procedures performed on the uterus and bladder and inchronic infected wounds such as ulcers. In these applications thereleased antibiotics is used to eradicate existing infection and inothers prophylactically.

Diabetic foot ulcers that are associated with osteomyelitis impose asubstantial burden on public and private payers in the United States,doubling care costs per patient compared with diabetic patients withoutfoot ulcers. Ulcer care adds around US $9 billion to $13 billion to thedirect yearly costs associated with diabetes itself(http://www.medscape.com/viewarticle/821908), and are due to increasedhospitalization costs as a result of foot amputations. The incidence ofnontraumatic lower extremity amputations (LEAs) has been reported to beat least 15 times greater in those with diabetes than with any otherconcomitant medical illness. LEA is less common but is an extremecomplication associated with diabetes and foot ulcer. In the U.S.,nearly 80,000 LEAs are performed on diabetics each year. In 2005, theoverall rate of hospital discharge for new LEA was about 4.3 per 1,000people with diabetes compared with a rate of about 0.3 per 1,000 in thegeneral population. The annual mortality rate for diabetic patients whohave an incident diabetic foot ulcer is about 11%; for those with anincident lower extremity amputation, about 22% (Margolis D J et al).

Antibiotics are most commonly incorporated into polymethylmethacrylate(PMMA) cement, which can then be formed into beads, molded to fit a bonedefect. The problem with PMMA beads is that they emit considerable heatupon polymerization which by itself might cause thermal damage to theantibiotic drug. In addition the heads are not degradable, and thepatient must undergo a second surgery to remove them before given a boneimplant. In addition, PMMA beads must be mixed with the desiredantibiotics in the surgical arena prior to the surgery. This is tediousand time consuming, and also incorporates a risk of improper mixingresulting in exposure to hyper or sub quantities of the antibiotic drug.To circumvent some of the problems outlined above with PMMA beadsdegradable bone substitutes have been developed. For example, CeramentBone Void Filler (Bonesupport, Sweden) is a degradable synthetic calciumsulfate bone substitute. In Europe it is sold also as a pre-mixedversion with antibiotics under the name Cerament G (contains gentamycin)and Cerament V (contains vancomycin). According to the manufacturer'sbrochure, the antibiotics elutes with a high initial peak that remainsabove the MIC for 28 days for staphylococcus aureus and pseudomonasaeruginosa. There is no evidence however of controlled release, theembedded antibiotic is released by diffusion according to concentrationgradient, this is less desired as the release profile might beinfluenced by the chemical and physical conditions at the site ofimplantation which are unique to each patient resulting in increasedvariability of the outcomes, reduced efficacy and predictability of thetreatment outcome. U.S. Pat. No. 9,180,137 B2 discusses calcium sulfatebased bone cement with the addition of antibiotics.

Other attempts to deliver antibiotics to an infected site includedpremixing the drug with fibrin glue. The intention is that the fibringlue serves as a delivery vehicle bringing the drug into the infectedsite, and retaining it there as the beads are entrapped in the hydrogel.Kara et al mixed antibiotics (moxifloxacin, lomefloxacin, vancomycin,and ceftazidime) with fibrin glue and measured the radius of inhibitionon petri plates covered with various bacterial strains. The drugs elutedup to 72 hours, and the elution did not show zero order kinetics butrather according to concentration gradient—most of the drugs werereleased during the first 24 hours. Tredwell et al mixed cefazolin withfibrin glue. Cefazolin was released in a controlled manner over 2 days,with most being released during the first day. Cashman et al blended theantibiotics cefazolin, fusidic acid or 5-fluorouracil into Vitageltissue sealant (fibrin glue with the addition of microfibrillarcollagen). The drugs were released in a controlled manner over 2-4 days.The above examples demonstrate that when drug are embedded in fibringlue, it diffuses out of the matrix according to its concentrationgradient, namely by a first order kinetics. This is because the drug ismuch smaller than the pores of fibrin glue and most other hydrogel, soit is free to diffuse out.

Penn-Barwell et al tested a bioabsorbable phospholipid gel, designatedDFA-02 containing 1.88% vancomycin and 1.68% gentamicin by weight in anopen fracture model in rats contaminated with Staphylococcus aureus. Theoutcome was better than PMMA beads containing the same drugs. However,concentrations of both antibiotics dropped rapidly within the first 48hours.

Local delivery of antibiotics is used to treat soft tissue infections aswell. For instance, gentamicin-itnpregnated collagen sponges have beentested as a bioabsorbable vehicle (CollaRx, Innocoll, Gallowston,Ireland). However, in a non-orthopedic clinical randomized controlledtrial the sponge group had a higher rate of surgical site infection andit was speculated that the antibiotics eluted faster than the spongedegraded, leaving foreign material in the wounds without antibiotics(Bennett-Guerrero et al).

For an efficient local antibiotic therapy it would be better to achievetight control over the release. A release with a zero order kinetics isthe gold standard of drug release. One way to achieve controlled releaseis to encapsulate the drug in microparticles (MPs) made from degradablehydrophobic materials, such as PLGA (polylactic glycolic acid) or PCL(polycaprolactone). The hydrophilic drug has to pass the hydrophobicmatrix on its way out of the MP, which retards its solubility anddiffusion resulting in zero order kinetics release, i.e. a constantrelease rate over time.

Setterstrom et al (U.S. Pat. No. 6,410,056) developed PLGA MPscontaining ampicillin or cefazolin to treat various infection models inrats including rat soft tissue wound infection model and rat fractionfixation model inoculated with Staphylococcus aureus, Streptococcuspyogenes or E. coli.

The challenge with using beads to treat local infections is how toretain them in the target site without their migration out of there. Dueto their small size, the beads will tend to migrate away, thus theeffective amount of antibiotic drug will be reduced. One approach wouldbe for the surgeon to compress the beads into a compact mass using asurgical tool. For example, Garvin et al teach using gentamycin loadedPLGA microspheres to treat osteomyelitis in a canine model. However, themicrospheres were compressed prior to implantation to a 5×15 millimetersrectangular shape implant, thus preventing migration of individual MPsaway from the defect site. A drawback of this approach is that thecompression reduces the effective surface area of the MPs, and by suchthe release profile of the drug is affected. In addition, compressingthe beads into a space or a cavity is time consuming, and the beads arelimited in their ability to penetrate narrow crevices, for example asthose found in bone, especially with large particles.

Treating soft tissue infections has always been a challenge because ofthe inaccessibility of orally or parenterally given antibiotic drugs tothe infected site or the toxicity associated with administering a highdose of antibiotics required to treat the infections. Infected diabeticfoot ulcers (DPI) are a good example of soft tissue infections that aredifficult to treat effectively, and the current therapies fail toprovide an adequate means of long term treatment. This is partly due tothe chronic nature of the wound and the persistence of the infectionwhich is exacerbated by factors such as impaired wound healing indiabetic patients and the geometrical dimensions of the ulcers, which inmany cases are deep and tunneled. The latter makes currently usedtreatments such as gauzes, bandages and dressings less efficient astheir contact area with the wound is limited to its upper external part.

Edwards et al evaluated several randomized controlled trials (RCTs) fordebridement of diabetic foot ulcers (DFU) and concluded that hydrogelsare significantly more effective than gauze or standard care in healingdiabetic foot ulcers. Certain groups took this approach further anddeveloped injectable hydrogels that are to be injected into the wounddepth. Marston et al treated patients having chronic DFU with aninjectable porcine collagen—derived matrix and reported a 72% reductionin wound size 2 weeks after injection. Campitiello et al treated 18patients with tunneled or cavity ulcers with an injectable matrixcomposed of crosslinked collagen and glycosaminoglycan which forms a gelin the body. According to the authors of the study 89% of the patientsshowed complete regeneration of the wound.

Antibacterial drugs have been combined in dry matrices as well fortreating soft tissue infections. For example, Gentamicin SurgicalImplant and CollaRx Gentamicin Topical (Innocoll Pharmaceuticals) areproducts made from a collagen sponge containing gentamicin, indicatedfor use in surgical site infections and diabetic foot infections (DFI),respectively. A clinical trial on 56 randomized patients with DFIshowedsome initial good results in patients who were treated with gentamicinimpregnated collagen sponge vs. placebo sponge vs. without sponge(Lipsky et al, 2012). However a much larger phase 3 study with thissponge (now called COGENZIA) did not achieve statistical significance inimproving clinical cure in diabetic foot infections (DFI). A similarproduct, COLLATAMP G is a lyophilized bovine Type I collagen matriximpregnated with gentamycin is indicated for surgical site infections.The manufacturer's web site shows the drug release profile, and it isclear that there was no controlled release profile of the antibiotics,and that the drug was above the MIC for only 7 days. These limitationsoften necessitate replacing the products up to several times a day, inorder to maintain the drug level above MIC for a prolonged time.

BRIEF SUMMARY OF THE INVENTION

The background art does not offer a solution to the problem of localizedtreatment with antibiotics that provides both excellent surface area fordrug release, and control over the timing and location of such release.While providing many small beads enables an excellent surface area, thebeads tend to migrate away from the location to be treated. A largerimplant that retains the beads at the target tissue solves the problemof bead migration but reduces the effective surface area for release andmay also result in certain tissues remaining untreated.

The present invention overcomes these drawbacks of the background art byproviding a composition and method for localized treatment of a tissuewith controlled drug release, which features fixated beads in a hydrogelmatrix. The matrix is preferably cross-linked gelatin that iscross-linked in situ, although optionally a different matrix could beused that is also capable of being cross-linked in situ. Without wishingto be limited to a closed list of benefits, the fixation prevents thebeads from migrating and retains their surface area while the beadsthemselves provide a means for controlled drug release. Preferably, thecontrolled drug release is also sustained.

The composition features encapsulating the drug in polymericmicroparticles to achieve zero order release kinetics, and embeddingthese particles in a hydrogel to allow easy access to the infected siteby virtue of their injectability as well as preventing their migrationout of the infected site due to hydrogel fixation to the target tissue.This approach of dispersing particulates in hydrogels has been named“plum pudding” by various research groups, and is a considered a subsetof composite gels. In addition the hydrogel itself preferably has thefollowing properties to achieve this goal: biocompatible, injectable,degradable (over a period of time longer than the desired releaseperiod), not interfering with the activity of the encapsulated drug andpromoting cellular growth. In addition the hydrogel preferably showsbioadhesive properties, because the adhesion to tissue is expected toprolong the residence time of the microparticles in the infected site.Another desired property is elasticity, as brittle hydrogel might breakdown or be subjected to mechanical erosion thus restricting theefficiency of the treatment.

The composition overcomes the drawbacks of previous such “plum pudding”attempts by providing a suitable hydrogel for the polymeric matrix,which preferably comprises cross-linked gelatin. The gelatin iscross-linked in situ, rather than being pre-cross linked, which providesa much better matrix for reasons described in greater detail below.Furthermore the composition itself is preferably bioadhesive, whichincreases the stability of application to the local tissue.

Other hydrogels have not been shown to be suitable for such a compositeapproach. For example, fibrin glue is not a suitable delivery vehiclefor drugs, as it is degraded quickly in vivo, and will usually be gonewithin a few days, long before the desired duration of 2-4 weeks of drugrelease.

US 20110038946 teach the use of injectable polyurethane scaffoldscontaining PLEA MPs with tobramycin. Polyurethane adhesives are notentirely biocompatible, especially when they are used as injectable, asthe components, namely polyisocyanates might diffuse away from theinjected mass prior to curing or in case of incomplete curing.

Foox et al teach the use of a gelatin-alginate hydrogel, crosslinkedwith EDC for antibiotics drug release. The matrix was loaded withantibiotics (clindamycin, ofloxacin, vancomycin). Only clindamycin wasfound to be inert toward the crosslinking reaction and did not decreasethe bonding strength of the bioadhesive. This was interpreted to be aresult of the EDC crosslinker interacting with carboxylic groups foundon ofloxacin and vancomycin, and demonstrates the importance of choosingan inert crosslinker for the hydrogel carrier matrix. 100% of theclindamycin contained in the gel was released after 4 hours, againdemonstrating the inability of gelatin hydrogels to retain embeddeddrugs without some sort of encapsulation in polymeric microparticles.

WO2014196943 teach the use of injectable hydrogel containing vancomycinMPs embedded in poloxamer. Poloxamers are the most widely used reversethermal gelation polymers, however the maximum duration of drug releasefrom poloxamers gel systems is limited by the influx of water whichdilutes the polymer below its critical gelation concentration such thatthe matrix loses gel-like properties (Hoare et al).

Gelatin has been used as a biomaterial for decades. It has been shown tobe safe, degradable, and biocompatible by numerous laboratories aroundthe world and is based on a vast accumulated clinical experience. Incontrast to hydrogels made from synthetic polymers such as poloxamersmentioned above or PEG, gelatin has a favorable tissue response andallow cellular in-growth, in part because it contains abundantArg-Gly-Asp (RGD) sequences which are the cell attachment sitesrecognized by many integrins. The mechanical properties of gelatinhydrogels can be enhanced by crosslinking, by either physical, chemicalor enzymatic means. Of note is enzymatic crosslinking of gelatin,induced by microbial transglutaminase, as described for example in U.S.Pat. Nos. 8,367,388 and 9,017,664, both owned in common with the instantapplication, both of which are hereby incorporated by reference as iffully set forth herein. This type of crosslinker is safer to use thanconventional means of crosslinking, i.e. glutaraldehyde or formaldehyde.

Another advantage of crosslinked gelatin hydrogels as carriers for drugdelivery is that it is injectable, and its degree of crosslinking can beadjusted to allow custom made degradation rate, as opposed to fibringlue, which is biocompatible but degrades within a few days, making itunsuitable to many applications where it is required to elute the drugat the infected site for a longer period. Finally, crosslinked gelatinhydrogel possesses favorable mechanical properties that are required toensure optimal performance at the site of implantation. First, gelatinis inherently bioadhesive, and demonstrates tackiness to varioustissues. The bonding strength of gelatin to tissues is due to thefunctional chemical groups on the tissue surface (e.g. lysines) whichcan interact with similar chemical groups on the gelatin molecule byvirtue of Van der Waals and hydrogen bonds. Crosslinking of gelatincontributes further to the bonding strength to tissues as a result ofcovalent bonds formed between the above mentioned chemical functionalgroups. Crosslinking also increases the cohesive bonds between gelatinchains by forming intermolecular covalent bridges. This contributes tothe cohesive strength of the matrix and the resulting tensile orcompression strength. The combination of adhesive strength and cohesivestrength ensures that the hydrogel remains attached at the targetinfected site for the duration required for delivering the drug.Overall, the above suggests that crosslinked gelatin matrices are idealfor drug delivery applications, when cross-linked in situ.

U.S. Pat. No. 8,138,157 describes antibiotic containing microparticles(for example made of PLGA.) in a gel, which is described as being madefrom Floseal (which contains gelatin). However, Floseal is made frompre-crosslinked gel particles. There is no curing process that forms agel in situ so the separate gel particles do not coalesce into acontinuous gel matrix. Therefore any drug eluting particles present inthe formulation might migrate out of the treatment site, unlike thesituation with in situ crosslinked gelatin matrix. In addition, Flosealis indicated as a hemostat. There is no evidence that it behaves as aglue or bioadhesive, therefore it is not expected to be suitable to beused in drug delivery applications where the drug carrier matrix isrequired to adhere to tissue at the target delivery site. Furthermore,this patent does not provide any experimental evidence to indicate theefficacy of this solution.

It would be advantageous to combine a wound healing promoting scaffoldor matrix with drug eluting properties, e.g. antibiotics to eradicateinfected deep tunneled or cavity ulcers. Cerament G or Cerament V elutegentamycin and vancomycin, respectively, but are constitute of bonecement and are therefore not suitable for soft tissue repair. There areseveral commercial topical wound dressing and gels with anti-microbialactivity, based on antiseptic agents (e.g. silver ions, iodine and PHMB)or antibiotics (e.g. bacitracin, mupirocin, retapamulin against grampositive bacteria; neomycin and silver sulfadiazine against gramnegative bacteria. These topical agents however do not possesscontrolled drug release properties and in addition are comprised ofsynthetic polymers with little to no biologic activity. A systematicreview of antimicrobial agents for chronic wounds (diabetic foot ulcers,pressure ulcers, chronic leg ulcers, etc.) concluded that few systemicagents improved outcomes (Lipsky et al, 2014). Therefore an improvementto the application and delivery system would clearly be of benefit intreating such chronic wounds.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention is herein described, by way of example only, withreference to the accompanying drawings. With specific reference now tothe drawings in detail, it is stressed that the particulars shown are byway of example and for purposes of illustrative discussion of thepreferred embodiments of the present invention only, and are presentedin order to provide what is believed to be the most useful and readilyunderstood description of the principles and conceptual aspects of theinvention. In this regard, no attempt is made to show structural detailsof the invention in more detail than is necessary for a fundamentalunderstanding of the invention, the description taken with the drawingsmaking apparent to those skilled in the art how the several forms of theinvention may be embodied in practice. In the drawings:

FIGS. 1A-1C show in vitro release of antibiotic drugs;

FIG. 2 shows release of ciprofloxacin MP embedded in enzymaticallycrosslinked gelatin matrix;

FIGS. 3A-3C show the anti-microbial activity of crosslinked gelatinhydrogel containing MPs with either gentamycin or vancomycin entrappedwithin the MPs; and

FIG. 4 shows mechanical testing of enzymatically crosslinked gelatinhydrogels.

FIG. 5 shows the size distribution of three different PLGA beadspreparations containing different antibiotic drugs.

DESCRIPTION OF AT LEAST SOME EMBODIMENTS

The present invention, in at least some embodiments, comprises acrosslinked gelatin hydrogel matrix containing microparticles. Theparticles contain a drug. The drug is released from the microparticles,for example and without limitation, optionally by diffusion or erosionmechanism. The rate of release is determined primarily by the materialfrom which the microparticle is comprised of, but also by otherparameters such as the type of drug, its solubility, the amount of theencapsulated drug. The product is preferably injectable, and undergoesin situ curing, which by the inherent adhesiveness to tissues fixatesitself onto the target tissue or anatomically defined space such ascavity or crevice.

The gelatin matrix is degradable, injectable and biocompatible. Thegelatin is made preferably from type A porcine skin, but can be madefrom bovine or fish gelatin as well. The gelatin has preferably a bloomof 100-300, more preferably 250-300, but optionally 100-250.

The gelatin matrix may optionally be crosslinked enzymatically, usingtransglutaminase, preferably from microbial source, but also optionallyusing mammalian transglutaminase, e.g. pig liver transglutaminase,Factor Xiii etc.

Optionally the gelatin matrix can be crosslinked using a chemicalcrosslinker such as glutaraldehyde or EDC.

The microparticles are manufactured using methods known to those skilledin the art. Non limiting examples include single emulsion method, doubleemulsion method, polymerization (normal or inter-facial), phaseseparation coacervation, spray drying and solvent extraction (forexample see Bansal et al).

Microparticles

The microparticles comprise one or more biocompatible polymers.Non-limiting examples of such biodegradable polymers include aliphaticpolymers (e.g. polylactic acid, polyglycolic acid, polycitric acid,polymalic acid, polycaprolactone), polycarbonates (e.g. polyethylenecarbonate, polyethylene propylene carbonate) and polyamine acids (e.g.poly-γ-benzyl-L-glutamic acid, poly-L-alanine, poly-γ-methyl-L-glutamicacid). These polymers may be homopolymers, copolymers of 2 or moremonomers, or a mixture of polymers. They may also be in the salt form.

Polylactic acid may be represented by the following structural formula:

wherein n for example can be any suitable integer between 10 and 250.Polylactic acid can be prepared according to any method known in thestate of the art. For example, polylactic acid can be prepared fromlactic acid and/or from one or more of D-lactide (i.e. a dilactone, or acyclic dimer of D-lactic acid), L-lactide (i.e. a dilactone, or a cyclicdimer of L-lactic acid), meso D,L-lactide (i.e. a cyclic dimer of D-,and L-lactic acid), and racemic D,L-lactide (racemic D,L-lactidecomprises a 1/1 mixture of D-, and L-lactide). Optionally the polylacticacid polymer comprises poly(L-lactic acid), poly(D,L-lactic acid) orpoly(D-lactic acid).

Polyglycolic acid may be represented by the following structuralformula:

wherein n for example can be any suitable integer between 10 and 250.

Polycaprolactone has the following structure:

wherein n for example can be any suitable integer between 10 and 250.

Polylactic glycolic acid copolymers have the following unit structure,which is preferably repeated a suitable number of times, for examplebetween 10 and 250 times:

Other non-limiting examples of suitable biocompatible polymers arepolystyrene, polyacrylic acid, polymethacrylic acid, polyamides,polyamino acids, silicon polymers, polyurethanes, etc.

Among these polymers, particularly preferred for use in this inventionare PLA (polylactic acid), PGA (polyglycolic acid) and PLGA (polylacticglycolic acid) copolymers, optionally in a ratio of lactic acid toglycolic acid in the copolymer from 20:80 to 80:20. Alternatively thepolymer is polycaprolactone.

The MPs (microparticles) size optionally ranges from 0.5 to 50 micron.

The MP containing the drug can be dispersed in the gelatin component,the enzyme component or both components of a liquid formulation ofcrosslinked gelatin. The amount of MP in the final formulation rangesbetween 1 mg/ml and 50 mg/ml, preferably between 5 mg/ml and 40 mg/ml,more preferably between 10 mg/ml and 30 mg/ml.

The dispersion of the MPs in one or more of the components of thegelatin matrix can be done during the manufacturing of the product orbefore use in the operating room. In the former case, the MPs are mixedwith one of the components, and are stored until use. Since in aqueousenvironment the encapsulated drug will start to diffuse out of the MPs,and since PLGA is subjected to hydrolysis in aqueous environments, thecomponent containing the MPs is better kept stored at a low temperature,refrigerated or frozen.

Alternatively, the MPs are kept dry, and are reconstituted with thegelatin or enzyme component just prior to use, in order to keep the MPstable. There are many technical solutions for reconstitution of the drypowder in a liquid formulation and these should be known to thoseskilled in the art. For example, RISPERDAL® CONSTA® (risperidone)Long-Acting Injection is a combination of extended-release microspheresfor injection and diluent for parenteral use. The microspheres areprovided dry in a vial, and reconstituted with the supplied diluentprior to injection inside the syringe. Alternatively, the microspherescan be reconstituted with the diluent during the assembly of a singlesyringe without a need for transfer between a syringe and a vial. Anexample is Lupron Depot (leuprolide acetate for depot suspension fortreatment of prostate cancer) which is supplied as a prefilled dualchamber syringe. This syringe contains powdered microspheres which whenmixed with diluent becomes a suspension. The suspension is thenadministered as a single intramuscular (IM) injection. A third variantis mixing by attaching syringe containing the diluent and a syringecontaining the MIP particles and passing the content between thesyringes for a number of times to make a homogenous suspension. Anexample for this variant is ELIGARD Injection (leuprolide acetate forinjectable suspension).

According to at least some embodiments, drug elution time is adjusted sothat the drug elutes from the microparticles over the course of 2 to 6weeks, preferably 2-5 weeks and more preferably 2-4 weeks, which is theamount of time required to eradicate the bacterial infection as anon-limiting example.

Various optional, non-limiting exemplary embodiments are now described,which may optionally also be combined with each other and/or with anyother embodiment or implementation as described herein. According to oneembodiment the gelatin sealant containing drug eluting MPs is injectedinto a cavity formed in bones following debridetnent of the infectedbone tissue in the case of osteomyelitis. After allowing a few minutesfor curing, the surgeon makes sure that the formulation has gelled andsolidified, before continuing with the surgery or closing the wound.Example 1 below shows that 3 different antibiotic drugs encapsulated inPLGA microparticles are released in a controlled manner following a zeroorder kinetics after an initial burst release. The PLGA MP containingciprofloxacin were embedded in an in situ cross-linkable gelatin matrixand the release rate was somewhat slower than MP alone, as a result ofthe additional diffusion barrier, but nevertheless the release wascontrolled with a zero order kinetics, and the drug eluted over thecourse of 2 weeks, which is the amount of time required to eradicate thebacterial infection.

Encapsulated Drug

The encapsulated drug may optionally comprise one or more ofantibiotics, analgesic, anti inflammatory, or anti-tumor drugs.

For all of the below antibiotics, optionally administration may be asthe pharmaceutically acceptable salts or hydrates, and/or combinationsof such antibiotics thereof.

Non-limiting examples of antibiotics include: an aminoglycosidicantibiotic, a glycopeptide antibiotic, ansamycins, carbacephems,carbapenems, cephalosporins, macrolides, penicillins, polypeptides,quinolones, sulfonamides, tetracyclines, lincosamides, nitrofurans,nitroimidazol es and mixtures thereof.

Non-limiting examples of aminoglycosidic antibiotics include etimicin,gentamicin, tobramycin, amikacin, netilmicin, dibekacin, kanamycin,arbekacin, sagamicin, isopamicin, sisomicin, neomycin, paromoycin,streptomycin, spectinomycin, micronomicin, astromicin, ribostamycin,pharmaceutically acceptable salts or hydrates, and combinations thereof.

Non-limiting examples of glycopeptide antibiotics include vancomycin,avoparcin, ristocetin, teicoplanin, telavancin, ramoplanin anddecaplanin, a derivative of vancomycin, avoparcin, ristocetin, orteicoplanin, pharmaceutically acceptable salts or hydrates, andcombinations thereof.

Non-limiting examples of carbacephem antibiotics include loracarbef.

Non-limiting examples of carbapenem antibiotics include ertapenem,meropenem, imipenem/cilastatin, panipenem, biapenem and tebipenem.

Non-limiting examples of cephalosporin antibiotics include cefadroxil,cefacetrile, cefalexin, cefaloglycin, cefalonium, cefaloridine,cefalotin, cefapirin, cefatrizine, cefazaflur, cefazedone, cefazolin,cefradine, cefroxadine, ceftezole, cefaclor, cefonicid, cefprozil,cefuroxime, cefamandole, cefuzonam, cefmetazole, cefotetan, cefixime,cefdinir, cefditoren, cefoperazone, cefotaxime, cefpodoxime,ceftazidime, ceftibuten, ceftizoxime, ceftriaxone, cefepime,ceftobiprole and cefoxitin.

Non-limiting examples of macrolide antibiotics include azithromycin,clarithromycin, erythromycin, fidaxomicin, dirithromycin, roxithromycin,troleandomycin, spectinomycin, telithromycin and spiramycin.

Non-limiting examples of penicillin antibiotics include amoxicillin,ampicillin, azlocillin, carbenicillin, cloxacillin, dicloxacillin,flucloxacillin, mezlocillin, meticillin, nafcillin, oxacillin,penicillin, piperacillin, and ticarcillin.

Non-limiting examples of quinolone antibiotics include ciprofloxacin,enoxacin, gatifioxacin, levofloxacin, lomefloxacin, moxifloxacin,norfloxacin, ofloxacin, trovafloxacin, grepafloxacin, sparfloxacin, andtemafloxacin.

Non-limiting examples of sulfonamide antibiotics include mafenide,sulfonamidochrysoidine, sulfacetamide, sulfadiazine, sulfamethizole,sulfanilimide, sulfasalazine, sulfisoxazole,trimethoprim-sulfamethoxazole, and cotrimoxazole.

Non-limiting examples of tetracycline antibiotics include doxycycline,minocycline, oxytetracycline, tetracycline.

Non-limiting examples of other suitable antibiotics include aztreonam, amonobactam antibiotic, amphenicol antibiotics such as chloramphenicoland thiamphenicol; ethambutol, fosfomycin, isoniazid, linezolid,mupirocin, platensimycin, pyrazinamide, quinupristin/dalfopristin,dapsone, clofazimine and trimethoprim.

Non-limiting examples of lincosamide antibiotics include lincomycin,clindamycin, and pirlimycin.

Non-limiting examples of ansamycin antibiotics include rifampicin.

Non-limiting examples of nitrofuran antibiotics include furazolidone,nitrofurantoin, nifurfoline, nifuroxazide, nifurquinazol, nifurtoinol,nifurzide, nitrofural, ranbezolid, furaltadone, furazidine, nifurateland nifurtimox.

Non-limiting examples of nitroimidazole antibiotics includemetronidazole, tinidazole, nimorazole, dimetridazole, pretomanid,ornidazole, megazol, azanidazole, benznidazole.

Non-limiting examples of anti-cancer antibiotics include geldanamycin,herbimycin, bleomycin.

In some cases one would want to encapsulate in microparticles drugs thatare non-soluble or poorly soluble in aqueous environment, and thereforeare not suitable for encapsulation using the most common techniquesknown in the art such as W/O/W double emulsion. Poor water solubilitywill result in low encapsulation efficiencies. For example lipophilicdrug molecules such as sterols and steroids, e.g. the anti-inflammatorydrug hydrocortisone are non-soluble in water. Benzocaine is a localanesthetic drug with very low water solubility. Acidic or basic drugs intheir free acid or free base form are poorly soluble, for exampleciprofloxacin in its free base form is insoluble in water, while thehydrochloride salt is soluble. In this case the microparticles will beprepared in alternative methods known to the skilled person in the art,such as oil/water emulsion, oil/oil emulsion, solid/oil/water technique,spray drying and more.

The drug content is optionally between 5-50% of the microparticleweight; alternatively, the polymer content is between 50-95% of themicroparticle weight. Preferably the drug content is between 5-30%, andmore preferably between 5-15%, of the microparticle weight.

Additional Hydrogel Embodiments

In another embodiment it is possible to add osteoconductive materials tothe gelatin matrix, in order to induce the formation of newly formedbone by facilitating cell infiltration, matrix deposition, and cellattachment in the cavity that will eventually replace the hydrogel.Example 4 shows an analysis of the mechanical properties of crosslinkedgelatin matrices that include hydroxyapatite (HA) compared to controlmatrix without HA. The addition of HA did not inhibit the crosslinkingof gelatin by transglutaminase, however it changed the mechanicalproperties of the gelatin matrix and made it more elastic.

In another embodiment, the crosslinked gelatin matrix containing the MPwith the antibiotics is used for prophylactic purposes, for example inorthopedic reconstructive surgeries where internal fixation devices areused (e.g. plates, rods, nails, screws) or in a total knee/hipreplacement. These surgeries carry a high risk of contamination,therefore applying an antibiotic eluting gelatin hydrogel at areas thatare at high risk for infection (e.g. the interface of the implant andthe bone, rough surfaces etc. that are prone to biofilm colonization)

In another embodiment the antibiotic eluting gelatin hydrogel can beplaced on in and around hernia meshes, which are susceptible tocontamination, and round the anchoring sutures or tacks used to fixatethe hernia mesh to the tissue.

Drug eluting gelatin hydrogels can be sprayed on the outer surface ofimplants to provide a controlled release of the relevant drug. Forexample, crosslinked gelatin hydrogel can be used to coat vascular stentand to release anti proliferative agents such as paclitaxel.

Antibiotics eluting gelatin gels can be used also for treatment andprophylaxis of soft tissue, e.g. diabetic foot ulcers, aortic and skingrafts.

In yet another embodiment the antibiotic eluting gelatin hydrogel can bemade as a dry formulation and used as a film or foam. This form has theadvantage that the microparticles containing the drug are alreadyembedded inside the cross-linkable gelatin matrix, so the reconstitutionstep by resuspension can be avoided. For foamed dry formulations the MPscan be integrated during the manufacturing of the dry formulation orafter the drying step. During the manufacturing process, the MPs can beadded either to the gelatin solution or to the enzyme solution or to thewet foam, followed by freeze drying of the wet foam. Alternatively, theMPs can be sprayed or sprinkled on the already dry foam. The MPs wouldadhere to the foam surface by electrostatic or Van der WaaIs forces.Alternatively, mixing the MPs with a volatile non aqueous solvent, thatdoes not dissolve the polymeric MPs, allows one to spray slurry of theMPs on the external surface of the foam, where the MPs will remainattached to that surface by virtue of capillary forces. Integration ofthe drug eluting MPs in a film is a straightforward process where theMPs are mixed with the gelatin matrix while at a liquid form, castedinto a suitable mold and allowed to dry.

Drug eluting dry film or foam can be used as a bandage for treatingburns (e.g eluting antibiotics), for wound healing, as anti-inflammatoryor anti-fibrosis treatment (e.g eluting NSAID), as a hemostat (e.g.eluting clotting factors) etc.

Antibiotic eluting hydrogel can be used for soft tissue repair. Forexample, for treating an infected diabetic foot ulcers (DFI), especiallyirregular shaped tunneling foot ulcers, an injectable matrix has anadvantage over a sponge or sheet form device as explained above. Thematrix will be injected to fill the tunneling wound so as to maximizethe contact area between the wound walls and the matrix, in order tofacilitate the diffusion of the drug from the matrix into the infectedwound bed. At the same time the gelatin matrix will serve as scaffoldfor tissue regeneration. This is based on the similarity of gelatin tocollagen, which is the main constituent of the extra cellular matrix.The other constituent are GAGS, which may be mimicked by addingpolysaccharides such as chitosan or hyaluronic acid.

EXAMPLES Example 1

Example 1 shows in vitro release of antibiotic drugs [gentamycin (FIG.1a ), vancomycin (FIG. 1b ) and ciprofloxacin (FIG. 1c )] frommicroparticles into PBS buffer. As shown, initially there was a burstrelease followed by a slower and constant release rate that followedzero order kinetics from 21 days up to at least 30 days.

PLGA (50:50) polymers, Resomer RG 503 H were purchased from EvonikIndustries. Ciprofloxacin HCl, vancomycin HCl, gentamicin sulfate salt,polyvinyl alcohol (PVA, MW˜31,000), dichloromethane (DCM), paraffin oil,acetonitrile (ACN), Span 80, hexane, monobasic sodium phosphatedihydrate, NaOH, ninhydrin, PBS, Mueller Hinton broth and LB agar werepurchased from Sigma Aldrich. All the materials were used as received.

Preparation of Antibiotic-Encapsulated PLGA BeadsVancomycin/Ciprofloxacin-Encapsulated PLGA Beads

Vancomycin/ciprofloxacin-encapsulated PLGA beads were prepared by adouble emulsion water-in-oil-in-oil (W/O1/O2) solvent evaporationtechnique. Briefly, 25 mg ciprofloxacin or 50 mg vancomycin weredissolved in 1 mL water (W) and 500 mg PLGA were dissolved in 5 mL DCM:ACN (1:1) mixture (O1). After pouring the W-phase into the O1-phase,emulsification was performed for 1 min using vortex. The first W/O1emulsion was progressively dispersed into 100 mL of paraffin oilcontaining 1% Span 80 (O2) using a 10 mL syringe and a 21G needle.During the addition, emulsification was performed using a magneticstirrer. This W/O1/O2 emulsion was stirred overnight to allow completesolvent evaporation and microsphere hardening.

The solid microspheres were recovered by filtration through a paperfilter (Whatman No 1), washed three times with hexane and three timeswith distilled water to remove non-encapsulated drug. The microsphereswere dried under vacuum at 35° C. overnight.

Gentamicin-Encapsulated PLGA Beads

Gentamicin-encapsulated PLGA beads were prepared by a double emulsionwater-in-oil-in-water (WO1/W2) solvent evaporation technique. Briefly,25 mg gentamicin were dissolved in 250 microliter water (W1) and 500 mgPLGA were dissolved in 5 mL DCM (O). After pouring the W1-phase into theO-phase, emulsification was performed for 1 min using vortex. The firstW1/O emulsion was progressively dispersed into 100 mL of a 1% (w/v)aqueous solution of PVA (W2) using a 10 mL syringe and a 21G needle.During the addition, emulsification was performed using an Ultra-Turraxhomogenizer (T-18, IKA). This W1/O/W2 emulsion was stirred overnight toallow complete solvent evaporation and microsphere hardening. The solidmicrospheres were collected by centrifugation at 10,000 g for 10 min,and washed three times with distilled water to remove non-encapsulateddrug. The microspheres were dried under vacuum at 35° C. overnight.

Drug Content and Encapsulation Efficiency

The amount of antibiotic was determined by dissolving 20 mg beads in 1mL NaOH 1 M at 37° C. After complete dissolution, 1 mL of HCl 1M wasadded to neutralize the pH. The ciprofloxacin and vancomycinconcentrations were determined using spectrophotometer at 275 and 280nm, respectively. A mixture of NaOH 1 M and HCl 1 M (1:1) was used as ablank.

The gentamicin concentration was determined by a colorimetric assay: 0.5mL of the gentamicin solution was mixed with 0.35 mL of sodium phosphatebuffer (50 mM, pH 7.4) and 0.15 mL of 1.25% ninhydrin solution. Thereaction occurred at 95° C. for 15 minutes and the tubes were thencooled in an ice-water bath for 10 min. The UV-visible spectra over thewavelength range of 200-700 nm were measured using the mixture ofninhydrin and the respective buffer solution at the appropriateconcentrations as the blanks. The gentamicin concentration wascalculated at the maximal absorbance (λmax˜315 nm).

The drug content and the encapsulation efficiency were calculated asfollows:

Drug content (%)=(Drug concentration in NaOH:HCl mixture [mg/mL]*2mL)/(Mass of beads [mg])*100

Theoretical drug content (%)=(Initial drug mass)/(Initial polymermass)*100

Encapsulation efficiency (%)=(Actual drug content)/(theoretical drugcontent)*100

Microsphere Size Analysis

The bead size distribution of the drug-encapsulated PLGA microsphereswas investigated using a microscope: Each objective of the microscopewas previously calibrated using a glass slide containing a ruler of 1 mmdivided into 10 μm-intervals (the microscope and accessories are fromDelta-Pix Company). the average bead diameters were calculated bymanually measuring the diameters of at least 20 beads from differentregions of microscope pictures. The average size of each preparation ofbeads is shown in FIG. 5.

FIG. 5A shows, in the left panel: light microscope image of PLGAmicroparticles containing ciprofloxacin; and in the right panel: sizedistribution of the microparticles. FIG. 5B shows, in the left panel:light microscope image of PLGA microparticles containing vancomycin; andin the right panel: size distribution of the microparticles. FIG. 5Cshows, in the left panel: light microscope image of PLGA microparticlescontaining gentamycin; and in the right panel: size distribution of themicroparticles.

In Vitro Drug Release Studies

The microspheres (25 mg of ciprofloxacin-encapsulated PLGA beads, 80 mgof gentamicin encapsulated PLGA beads, 40 mg of vancomycin-encapsulatedPLGA beads) were placed into glass vials filled with 10 mL solution (PBSfor vancomycin and ciprofloxacin-encapsulated PLGA beads and sodiumphosphate buffer for gentamicin encapsulated PLGA beads). The vials wereplaced in an orbital shaker incubator at 37° C., where they were shakenat 120 rpm. For ciprofloxacin and vancomycin, once a day, 1.5 mL of thesuspension was centrifuged and 1 mL of the supernatant was taken tospectrophotometer to measure the drug concentration. Finally, the 1.5 mLof suspension were returned back into the glass vials. For gentamicin,the reaction with ninhydrin is irreversible. 0.5 mL of the solution wasreplaced each day with fresh sodium phosphate buffer to maintain aconstant volume.

Example 2

Example 2. shows release of ciprofloxacin from PLGA microparticlesembedded in enzymatically crosslinked gelatin matrix. The release of thedrug is somewhat slower When the MPs were embedded in gelatin matrixcompared to free MPs (FIG. 2), this may be explained by the additionaldiffusion that is required from the drug inside the gelatin matrix afterit has eluted from the MPs. Entrapment of microparticles inenzymatically crosslinked gelatin hydrogel was performed as follows.

160 mg of ciprofloxacin-encapsulated PLGA beads were added to 2.7 gr ofenzyme solution. This solution was mixed with 5.0 gr of gelatinsolution. 0.25 gr of the mixture was cast in a glass vial, and curingoccurred at 37° C. for 15 min. 5 mL of PBS was added to the vial to washthe gel. An additional 5 mL of PBS was added and the vial was placed inan orbital shaker incubator at 37° C., where it was shaken at 120 rpm.Once a day, 1.5 mL of the cured gel extract was centrifuged and 1 mL ofthe supernatant was taken to spectrophotometer to measure the drugconcentration. After measurement, the 1.5 mL extract was returned backinto the glass vials. crosslinked gelatin without beads was castedaccording to the same procedure and the extract was used as blank.

Example 3

Example 3 shows the anti-microbial activity of crosslinked gelatinhydrogel containing MPs with either gentamycin or vancomycin entrappedwithin the MPs. The bacteria used was Bacillus subtilis, which serves asa model microorganism for grain positive bacteria. Gels that wereincubated in saline for 14 days still had enough drug remaining withinthe matrix to induce bacteria killing, as can be seen from the ringaround the gel, in agar diffusion (Kirby-Bauer) assay (FIG. 3A) or theconcentration of the eluted antibiotic drug which was considerably aboveMIC throughout the study (FIG. 3B). The data is summarized in FIG. 3C.

Antibacterial Activity Against bacillus subtilis (ATCC 6633,Microbiologics #0486)

6 discs of 0.2 gr crosslinked gelatin containing 2%vancomycin/gentamicin-encapsulated PLGA beads were casted in plasticmold of 12 mm diameter. After 15 min of curing at 37° C., the gels wereseparately placed in glass vial filled with 1.5 mL sodium phosphatebuffer. The vials were placed in an incubator at 37° C. After 1, 2, 4,7, 11 and 14 days, the gel was taken out and the hydrogel extract wasfrozen until test.

The antibacterial activity of the hydrogel discs extracts was studied byemploying a microdilution method (FIG. 3b ). Plates were prepared understerile conditions. 100 μL of test materials were pipetted into thefirst column of the sterile 96-well plate. To all other wells 50 μL ofsaline was added. Serial dilutions were performed using a multichannelpipette. Tips were discarded after use such that each well had 50 μL ofthe test material in serially descending concentrations. Then, 50 μL ofMuller Hinton (MH) broth was added to each well followed by 100 μL ofbacterial suspension (prepared by growing bacteria in MH broth untilOD₆₆₀ of 0.1, then diluted 100× fold in fresh MH).

Each plate had a set of controls: a column with all the solutions withthe exception of the bacterial solution adding 50 μL of nutrient brothinstead, and a column without antibiotic. The two last rows were usedfor the determination of the MX: a gentamicin or vancomycin solutionwith a concentration of 64 mg/mL and 60 μg/mL, respectively, was addedto the first wells and serial dilutions were performed. The plates wereprepared in duplicate, and placed overnight in an orbital shakerincubator at 37° C. where a horizontal shake was performed at 120 rpm.

After 24 hours, the OD of each well was measured at 600 nm todeterminate the presence or absence of bacterium. The lowestconcentration at which opaque color was detected (OD 0.25) was taken asthe MIC value.

Agar Disk-DIFFUSION method (FIG. 3 a)

3 discs of 0.2 gr crosslinked gelatin containing 2%vancomycin/gentamicin-encapsulated PLGA beads were casted as previouslyreported. 3 additional discs without beads were also casted and used asnegative control. Filters containing 30 μg antibiotics (gentamicin orvancomycin) were used as positive controls.

The gel discs with and without beads and the filter containingantibiotics were placed in LB agar plates on which 100 μl of bacteriumsuspension had been evenly spread. The petri dishes were placed in anorbital shaker incubator at 37° C. where a horizontal shake wasperformed at 120 rpm.

Example 4

Example 4 shows mechanical testing of enzymatically crosslinked gelatinhydrogels. Hydroxyapatite was added to the gel, a control group wastested without hydroxyapatite (HA). The gels were analyzed using anInstron texture analyzer, and the tensile stress and strain at break wasdetermined for each group (FIG. 4). The results show that the inpresence of HA the crosslinked gel became more elastic, as isdemonstrated by the reduced Young's modulus and increased strain atbreak.

Preparation of a 16% Gelatin Containing 1.6% Hydroxyapatite

Materials: Gelatin Type A (Gelita) Tween 20, microbial transglutaminasesolution 50 U/mL, hydroxyapatite particles 5 microns in size (SigmaAldrich).

Procedure:

1.2 gr TWEEN 20 was diluted in 10 mL water. The solution was stirred fora few minutes. That solution was added to 284.3 g water and 57 g gelatinduring heating and stirring until complete dissolution was achieved.

323 mg of hydroxyapatite (10% of the gelatin mass) was added to 20 g ofthe precedent gelatin-tween solution. The final concentrations ofgelatin, hydroxyapatite and tween 20 are 16%, 1.6% and 0.33%,respectively.

An additional solution was prepared without hydroxyapatite and was usedas control.

8 dog bone shaped gels from each solution were casted in Teflon coatedmolds. They were placed in an incubator at 37° C. for 30 min, and thentransferred to a dish plate with 20 mL saline for 24 hours.

Tensile stress-strain tests were conducted (Instron 3345) at 0.5 mm/sec,at room temperature on swollen samples (FIG. 4). The measurements werecarried out until the gels were torn. The tensile Young's modulus, E,was determined from the linear slope, at 10 to 30% elongation, of thetensile stress-strain curve.

REFERENCES Non Patent Literature

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It is appreciated that certain features of the invention, which are, forclarity, described in the context of separate embodiments, may also beprovided in combination in a single embodiment. Conversely, variousfeatures of the invention, which are, for brevity, described in thecontext of a single embodiment, may also be provided separately or inany suitable sub-combination.

Although the invention has been described in conjunction with specificembodiments thereof, it is evident that many alternatives, modificationsand variations will be apparent to those skilled in the art.Accordingly, it is intended to embrace all such alternatives,modifications and variations that fall within the spirit and broad scopeof the appended claims. All publications, patents and patentapplications mentioned in this specification are herein incorporated intheir entirety by reference into the specification, to the same extentas if each individual publication, patent or patent application wasspecifically and individually indicated to be incorporated herein byreference. In addition, citation or identification of any reference inthis application shalt not be construed as an admission that suchreference is available as prior art to the present invention.

What is claimed is:
 1. A composition, comprising a hydrogel matrix andmicroparticles within said matrix, said matrix comprising across-linkable protein and a cross-linking agent, wherein saidcross-linking agent is able to cross-link said cross-linkable protein,wherein said microparticles comprise a drug; wherein said cross-linkableprotein comprises gelatin and wherein said cross-linking agent comprisestranglutaminase; wherein said cross-linking of said cross-linkableprotein causes said cross-linkable protein to become fixated onto atissue or anatomically defined space.
 2. The composition of claim 1,wherein said drug is released from the microparticles, at a rate ofrelease determined according to at least one characteristic of amaterial of said microparticles and according to at least onecharacteristic of the drug.
 3. The composition of claim 2, wherein saidaverage rate of release is under 5% per day.
 4. The composition of claim3, wherein said average rate of release is under 4% per day.
 5. Thecomposition of claim 4, wherein said average rate of release is under 3%per day.
 6. The composition of claim 5, wherein said average rate ofrelease is under 2% per day.
 7. The composition of claim 6, wherein saidaverage rate of release is under 1% per day.
 8. The composition of anyof the above claims, wherein said cross-linking agent cross-links saidcross-linkable protein only in situ.
 9. The composition of any of theabove claims, wherein said gelatin is made from t type A porcine skin,bovine or fish gelatin.
 10. The composition of claim 9, wherein saidgelatin has a bloom of 100-300.
 11. The composition of claim 10, whereinsaid gelatin has a bloom of 100-250.
 12. The composition of claim 11,wherein said gelatin has a bloom of 250-300
 13. The composition of anyof claims 9-12, wherein said transglutaminase is microbial or mammalian.14. The composition of claim 13, wherein said transglutaminase ismicrobial.
 15. The composition of any of the above claims, wherein saidmicroparticles comprise a biodegradable polymer selected from the groupconsisting of: an aliphatic polymer, a polycarbonate polymer and apolyamino acid polymer.
 16. The composition of claim 15, wherein saidaliphatic polymer is selected from the group consisting of polylacticacid, polyglycolic acid, polycitric acid, polymalic acid, andpolycaprolactone.
 17. The composition of claim 15, wherein saidpolycarbonate polymer is selected from the group consisting ofpolyethylene carbonate and polyethylene propylene carbonate.
 18. Thecomposition of claim 15, wherein said polyamino acid polymer is selectedfrom the group consisting of poly-γ-benzyl-L-glutamic acid,poly-L-alanine, and poly-γ-methyl-L-glutamic acid.
 19. The compositionof any of claims 15-18, wherein the biodegradable polymer comprises ahomopolymer, copolymer of 2 or more monomers, or a mixture of polymers.20. The composition of claim 19, wherein the biodegradable polymer is inthe salt form.
 21. The composition of any of the above claims, whereinsaid microparticles comprise one or more of PLA (polylactic acid), PGA(polyglycolic acid), polycaprolactone and PLGA (polylactic glycolicacid) copolymer.
 22. The composition of claim 21, wherein said PLGA isin a ratio of lactic acid to glycolic acid in the copolymer from 20:80to 80:20.
 23. The composition of any of the above claims, wherein saiddrug comprises one or more of antibiotics, analgesic drugs,anti-inflammatory drugs, or anti-tumor drugs.
 24. The composition ofclaim 23, wherein said antibiotic is selected from the group consistingof an aminoglycosidic antibiotic, a glycopeptide antibiotic, ansamycins,carbacephems, carbapenems, cephalosporins, macrolides, penicillins,polypeptides, quinolones, sulfonamides, tetracyclines, I incosamides,nitrofurans, nitroimidazoles and mixtures thereof.
 25. The compositionof claim 24, wherein said aminoglycosidic antibiotic is selected fromthe group consisting of etimicin, gentamicin, tobramycin, amikacin,netilmicin, dibekacin, kanamycin, arbekacin, sagamicin, isopamicin,sisomicin, neomycin, paromoycin, streptomycin, spectinomycin,micronotnicin, astromicin, ribostamycin, pharmaceutically acceptablesalts or hydrates, and combinations thereof
 26. The composition of claim24, wherein said glycopeptide antibiotic is selected from the groupconsisting of vancomycin, avoparcin, ristocetin, teicoplanin,telavancin, ramoplanin and decaplanin, a derivative of vancomycin,avoparcin, ristocetin, or teicoplanin, pharmaceutically acceptable saltsor hydrates, and combinations thereof.
 27. The composition of claim 24,wherein said carbacephem antibiotic is loracarbef.
 28. The compositionof claim 24, wherein said carbapenem antibiotic is selected from thegroup consisting of ertapenem, meropenem, imipenem/cilastatin,panipenem, biapenem and tebipenem.
 29. The composition of claim 24,wherein said cephalosporin antibiotic is selected from the groupconsisting of cefadroxil, cefacetrile, cefalexin, cefaloglycin,cefalonium, cefaloridine, cefalotin, cefapirin, cefatrizine, cefazaflur,cefazedone, cefazolin, cefradine, cefroxadine, ceftezole, cefaclor,cefonicid, cefprozil, cefuroxime, cefamandole, cefuzonam, cefmetazole,cefotetan, cefixime, cefdinir, cefditoren, cefoperazone, cefotaxime,cefpodoxime, ceftazidime, ceftibuten, ceftizoxime, ceftriaxone,cefepime, ceftobiprole and cefoxitin.
 30. The composition of claim 24,wherein said macrolide antibiotic is selected from the group consistingof azithromycin, clarithromycin, erythromycin, fidaxomicin,dirithromycin, roxithromycin, troleandomycin, spectinomycin,telithromycin and spiramycin,
 31. The composition of claim 24, whereinsaid penicillin antibiotic is selected from the group consisting ofamoxicillin, ampicillin, azlocillin, carbenicillin, cloxacillin,dicloxacillin, flucloxacillin, mezlocillin, meticillin, nafcillin,oxacillin, penicillin, piperacillin, and ticarcillin.
 32. Thecomposition of claim 24, wherein said quinolone antibiotic is selectedfrom the group consisting of ciprofloxacin, enoxacin, gatifloxacin,levofloxacin, lomefloxacin, moxifloxacin, norfloxacin, ofloxacin,trovafloxacin, grepafloxacin, sparfloxacin, and temafloxacin.
 33. Thecomposition of claim 24, wherein said sulfonamide antibiotic is selectedfrom the group consisting of mafenide, sulfonamidochrysoidine,sulfacetamide, sulfadiazine, sulfamethizole, sulfanilimide,sulfasalazine, sulfisoxazole, trimethoprim-sulfamethoxazole, andcotrimoxazole.
 34. The composition of claim 24, wherein saidtetracycline antibiotic is selected from the group consisting ofdoxycycline, minocycline, oxytetracycline and tetracycline.
 35. Thecomposition of claim 24, wherein said antibiotic is selected from thegroup consisting of aztreonam, chloramphenicol, thiamphenicol;ethambutol, fosfomycin, isoniazid, linezolid, mupirocin, platensimycin,pyrazinamide, quinupristin/dalfopristin, dapsone, clofazimine andtrimethoprim.
 36. The composition of claim 24, wherein said lincosamideantibiotic is selected from the group consisting of lincomycin,clindamycin, and pirlimycin.
 37. The composition of claim 24, whereinsaid ansamycin antibiotic is rifampicin.
 38. The composition of claim24, wherein said nitrofuran antibiotic is selected from the groupconsisting of furazolidone, nitrofurantoin, nifurfoline, nifuroxazide,nifurquinazol, nifurtoinol, nifurzide, nitrofural, ranbezolid,furaltadone, furazidine, nifuratel and nifurtimox.
 39. The compositionof claim 24, wherein said nitroimidazole antibiotic is selected from thegroup consisting of metronidazole, tinidazole, nimorazole,dimetridazole, pretomanid, ornidazole, megazol, azanidazol andbenznidazole.
 40. The composition of claim 24, wherein said antibioticis selected from the group consisting of vancomycin and gentamycin. 41.The composition of any of claims 24-40, wherein administration of thedrug is as a pharmaceutically acceptable salt or hydrate, and/or acombination of said antibiotics.
 42. The composition of claim 23,wherein said anti-cancer drug is selected from the group consisting ofgeldanamycin, herbimycin and bleomycin.
 43. The composition of any ofthe above claims, wherein said drug content is between 5-50% of themicroparticle weight.
 44. The composition of claim 34, wherein the drugcontent is between 5-30% of the microparticle weight.
 45. Thecomposition of claim 44, wherein the drug content is between 5-15% ofthe microparticle weight.
 46. The composition of any of the aboveclaims, wherein a polymer content of said particles is between 50-95% ofthe microparticle weight.
 47. The composition of any of the aboveclaims, wherein a size range of said microparticles is 0.5-50 microns.48. The composition of claim 47, wherein said size range is 1-30microns.
 49. The composition of any of the above claims, wherein saidmicroparticles containing the drug are dispersed in the proteincomponent, the cross-linking agent component or both.
 50. Thecomposition of claim 49, wherein an amount of microparticles in eachcomponent ranges between 10 mg/ml and 80 mg/ml.
 51. The composition ofclaim 50, wherein an amount of microparticles in the final formulationfollowing the mixing of said components ranges between 10 mg/ml and 80mg/ml.
 52. The composition of claim 50 or 51, wherein said amount rangesbetween 20 mg/ml and 70 mg/ml.
 53. The composition of claim 52, whereinsaid amount ranges between 30 mg/ml and 60 mg/ml.
 54. The composition ofany of the above claims, wherein drug elution time from themicroparticles is adjusted so that the drug elutes from themicroparticles over the course of 2 to 6 weeks, alternatively 2-5 weeksor 2-4 weeks.